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Pediatr Blood Cancer

Langerhans Cell Histiocytosis (LCH): Guidelines for Diagnosis, Clinical Work-Up,


and Treatment for Patients Till the Age of 18 Years

Riccardo Haupt, MD,1 Milen Minkov, MD,2 Itziar Astigarraga, MD,3 Eva Schäfer, MSc,4 Vasanta Nanduri, MD,5
Rima Jubran, MD,6 R. Maarten Egeler, MD, PhD,7 Gritta Janka, MD,8 Dragan Micic, MD,9
Carlos Rodriguez-Galindo, MD,10 Stefaan Van Gool, MD,11 Johannes Visser, MBChB,12
Sheila Weitzman, MD,7Jean Donadieu, MD, PhD4* and for the Euro Histio Network

These guidelines for the management of patients up to 18 years publications have been ranked according to evidence based medi-
with Langerhans cell histiocytosis (LCH) have been set up by a cine and when there was a lack of published data, consensus
group of experts involved in the Euro Histio Net project who par- between experts was sought. Guidelines for diagnosis, initial clini-
ticipated in national or international studies and in peer reviewed cal work-up, and treatment and long-term follow-up of LCH
publications. Existing guidelines were reviewed and changed where patients are presented. Pediatr Blood Cancer
new evidence was available in the literature up to 2012. Data and ß 2012 Wiley Periodicals, Inc.

Key words: clinical work-up; diagnosis; follow-up; guidelines; Langerhans cell histiocytosis; therapy

INTRODUCTION Scientific articles published in peer-reviewed journals up to


January 2012 were systematically reviewed. In addition to the
Langerhans cell histiocytosis (LCH) is a heterogeneous dis- medical literature, the following guidelines are a synthesis of
ease, characterized by accumulation of dendritic cells with fea- different international and national guidelines and recommenda-
tures similar to epidermal Langerhans cells in various organs. Any tion documents.
organ or system of the human body can be affected, but those Evidence was ranked in four levels [1,2]: (A) meta-analyses,
more frequently involved are the skeleton (80% of cases), the skin high quality systematic reviews, or randomized controlled trials
(33%), and the pituitary (25%). Other organs involved are the with a low risk of bias; (B) systematic reviews of case–control or
liver, spleen, the hematopoietic system and the lungs (15% cohort studies; (C) non-analytic studies; for example, case reports,
each), lymph nodes (5–10%), and the central nervous system case series, small retrospective studies; (D) expert opinion. Level
excluding the pituitary (2–4%). The clinical course may vary of agreement between experts and data was ranked in three clas-
from a self-limiting disease to a rapidly progressive one that ses: (2) general agreement between all experts or between avail-
might lead to death. Between 30% and 40% of patients may able studies; (1) discussed recommendation, but no formal
develop permanent adverse sequelae. Treatment options vary objections between experts or mild difference between studies,
depending on the extent of the disease and the severity at onset. without contradiction for the main endpoint; (0) divergence of
Response to front-line treatment is an important information to opinion or contradictory results for the main endpoint.
adapt the therapeutic strategy. As LCH is a rare disease, only a
limited number of large surveys or of randomized clinical trials
are available in the literature and many aspects of the manage- Additional Supporting Information may be found in the online version
ment of patients remain obscure or controversial. The presented of this article.
guidelines are based on published evidence and the clinical ex- Abbreviations: LCH, Langerhans cell histiocytosis; MRI, magnetic
pertise of the authors. They are intended to provide guidance with resonnance imaging; CNS, central nervous system; DI, diabetes insip-
respect to diagnosis and clinical work-up of LCH occurring in idus; MS-LCH, multi system Langerhans cell histiocytosis; SS-LCH,
patients <18 years old. The recommendations can neither replace single system Langerhans cell histiocytosis; RO, risk organs.
1
the physician’s own professional judgement nor consider all spe- Department of Hematology and Oncology, Epidemiology and Bio-
cial clinical circumstances which may apply to individual cases. statistics Section, Istituto G. Gaslini, Genova, Italy; 2Children’s Can-
cer Research Institute, St. Anna Children’s Hospital, Vienna, Austria;
3
Hospital Universitario Cruces Barakaldo, Barakaldo, Spain; 4Refer-
METHODS ence Centre for Histiocytosis at Hopital Trousseau, Assistance Pub-
lique – Hopitaux de Paris, France; 5Watford General Hospital,
This document is derived from the project Euro Histio Net Watford, UK; 6Children’s Hospital of Los Angeles, Los Angeles,
2008, a reference network (www.eurohistio.net) for LCH and California; 7Hospital for Sick Children, Toronto, Ontario, Canada;
8
associated syndromes in the European Union which received University Medical Center Hamburg-Eppendorf, Hamburg,
funding within the framework of the Public Health Program. Germany; 9Mother and Child Health Institute of Serbia ‘‘Dr Vukan
The guidelines were designed and established by European and Cupic,’’ Belgrade, Serbia; 10Dana Farber Cancer Institute, Children’s
Hospital Boston, Boston, Massachusetts; 11University Hospital Gas-
North American physicians considered to be experts in the field of
thuisberg, Leuven, Belgium; 12University Hospitals of Leicester,
pediatric histiocytic disorders. They are active members of the Leicester Children’s Hospital, Leicester, UK
international medical society of histiocytoses ‘‘Histiocyte Socie-
ty’’ (HS), of the European national societies of Hematology/ Conflict of interest: Nothing to declare.
Oncology, and of their respective national groups for the study *Correspondence to: Jean Donadieu, MD, PhD, Service d’Hémato
and treatment of these diseases. The guidelines have been devel- Oncologie Pédiatrique, Hopital Trousseau, 26 avenue du Dr Netter,
oped for use as recommended practice in the evaluation and F 75012 Paris, France. E-mail: jean.donadieu@trs.aphp.fr
treatment of children and teenagers up to 18 years with LCH. Received 13 May 2012; Accepted 18 September 2012
ß 2012 Wiley Periodicals, Inc.
DOI 10.1002/pbc.24367
Published online in Wiley Online Library
(wileyonlinelibrary.com).
2 Haupt et al.

TABLE I. Differential Diagnosis for Manifestations of Langerhans Cell Histiocytosis

Involvement Manifestation Possible other condition


Skin Vesicles and bullae (most common in early infancy) Erythema toxicum
Herpes simplex
Varicella
Dermatitis (most frequently scalp, diaperarea, Seborrheic dermatitis (eczema; usually no petechiae
or axilla, may occur up to late infancy) and marked scaling)
Nodules Mastocytosis
Juvenile xanthogranuloma
Neuroblastoma
Infant leukemia
Pruritus Scabies (other family members may be affected)
Petechiae
Bone Vertebra plana Ewing sarcoma
Septic osteomyelitis
Chronic relapsing multifocal osteomyelitis (CRMO)
Leukemia
Lymphoma
Aneurysmal bone cyst
Juvenile xanthogranuloma
Myeloma (only described in adults)
Osteoporosis
Temporal bone Chronic otitis media
Mastoiditis
Cholesteatoma
Soft tissue sarcoma
Orbit Acute infection (preseptal cellulitis)
Dermoid cyst
Rhabdomyosarcoma
Neuroblastoma
Erdheim–Chester disease
Pseudoinflammatory tumor
Other lytic lesions of the long bones Septic osteomyelitis
Chronic recurrent multifocal osteomyelitis (CRMO)
Aneurysmal bone cyst
Bone angiomatosis (Gorham disease)
Fibrous dysplasia
Atypical mycobacterial infection
Osteogenic sarcoma
Ewing’s sarcoma
Lung In particular systemic symptoms Pneumocystis jirovecii cavitated infection
and cavitated pulmonary nodules Mycobacterial or other pulmonary infections
Sarcoidosis
Bronchiolar–alveolar carcinoma (only described in adults)
Lymphangio–Leiomyosarcoma (only described in young adult women)
Septic emboli
Liver Jaundice with direct hyperbilirubinemia Chronic destructive cholangitis
Hypoalbuminemia Metabolic disease
Hepatitis
Neoplasia obstructing biliary tract
Inherited deficient conjugation of bilirubin
Toxic (Reye syndrome)
Chronic inflammatory bowel disease
Neonatal hemochromatosis
Endocrine Diabetes insipidus Central nervous sysytem germ cell tumor
Hypophisitis

Langerhans Cell Histiocytosis Diagnosis clinicopathologic and should only be made in the appropriate
Since LCH may affect any organ or system of the body, the clinical setting to prevent a misdiagnosis in the presence of nor-
condition should be considered whenever suggestive clinical man- mal reactive Langerhans cells, particularly in regional lymph
ifestations occur in the skin, bone, lung, liver, or CNS. Table I nodes. In addition to clinical and radiological features, LCH
shows a list of differential diagnoses to be considered depending diagnosis should always be based on histological and immuno-
on presenting complaints, signs, or symptoms. The diagnosis is phenotypic examination of lesional tissue (agreement: 2), that
Pediatr Blood Cancer DOI 10.1002/pbc
Guidelines for Langerhans Cell Histiocytosis 3

should be taken from the most easily accessible, yet representative TABLE II. Laboratory and Radiographic Evaluation of Children
lesion. With LCH
There is a well defined histologically characteristic appearance
of the LCH lesions on hematoxylin and eosin stained sections, but Evaluation
positive CD1a and/or CD207 (Langerin) staining of the lesional Full blood count
cells is required for a definitive diagnosis [3–6] (agreement: 2). Hemoglobin
Electron microscopy is no longer needed (agreement: 2), since it White blood cell and differential count
has been shown that the expression of Langerin correlates with Platelet count
the ultrastructural presence of Birbeck granules. Diagnostic con- Blood chemistry
firmation may be a challenge in some circumstances (e.g., liver Total protein
specimens), where Birbeck granules are not present and CD1a Albumin
and/or Langerin may be negative because LCH cells have regress- Bilirubin
ALT (SGPT)
ed after having caused sclerosing cholangitis and Cirrhosis [7].
AST (SGOT)
In rare cases the risk of biopsy may outweigh the need for a gGT
definitive diagnosis, and therefore the risk/benefit ratio should be Creatinine
carefully assessed. This is the case in patients with isolated Electrolytes
involvement of a vertebral body without an adjacent soft tissue Erythrocyte sedimentation rate (ESR)
component, as in case of vertebra plana, or with isolated involve- Abdominal ultrasound (in particular for young children)
ment of the odontoid peg. If the decision to avoid or postpone a Size and structure of liver and spleen
biopsy is made, every effort should be made to rule out other Abdominal lymph-nodes
conditions that might lead to a similar radiological finding Coagulation studies
(Table I). INR/PT
APTT/PTT
Patients without a histologically confirmed diagnosis need to
Fibrinogen/factor I
be carefully monitored by appropriate imaging for at least the Chest Radiograph (CXR)
next 6 months in order to reassess the need for biopsy and its Skeletal radiograph surveya,b
justification, in order to exclude a malignancy.
ALT (SGPT), alanine transaminase (serum glutamic pyruvic transam-
inase); APTT/PTT, activated partial thromboplastin time/partial
Pretreatment Clinical Evaluation
thromboplastin time; AST (SGOT), aspartate transaminase (serum
Once the diagnosis of LCH has been ascertained it is impor- glutamic oxaloacetic transaminase); gGT, gamma-glutamyltransfer-
tant to collect further baseline information in order to decide on a ase; INR/PT, international normalized ratio/prothrombin time; MRI,
therapeutic approach. A complete history should include special magnetic resonance imaging; PET, positron emission tomography;
Tc, technetium. aNote that other imaging techniques as bone Tc
reference to the nature and duration of symptoms. Specific symp-
scan, PET scan, or MRI are not an alternative to the standard skeletal
toms to be sought are: pain, swelling, skin rashes, otorrhea, fever, survey. The real value of these images in LCH is still under study. In
loss of appetite, diarrhea, poor weight gain, growth failure, poly- particular information from bone scan should not be considered for
dipsia, polyuria, respiratory symptoms, irritability, behavioral, and evaluation of disease extent and decision-making. PET scan has prov-
neurological changes. A detailed examination should be per- en to be the most sensitive functional test used in the identification of
formed at the onset and at each follow-up visit. Currently there LCH lesions and in evaluating patient response to therapy. However,
is no specific biological marker of disease activity, however, there it is currently expensive, exposes the patient to a significant radiation
is a general agreement (agreement: 2) that biochemical and imag- dose and is not widely available [56]. bIt is not recommended to
ing evaluation at diagnosis and at disease reactivation should change the method of bone evaluation (skeletal radiograph), as it
include the mandatory investigations listed in Table II. Certain may lead to discrepancy between assessments. It is important also
to consider the ALARA principle (as low as reasonably achievable)
scenarios might require additional testing; the recommended
for ionizing radiation and, if possible, during follow up, limit the
laboratory investigations, imaging, or specialized clinical assess- evaluation to the anatomic region initially involved.
ments upon specific indication are shown in Table III; the detailed
protocol for head MRI is provided in (Supplemental Appendix I).
the absence of involvement of other risk organs, lung disease is
Defining Organ Involvement, Risk Organs, only in exceptional cases the ultimate cause of death [12,13], and
this usually occurs through ‘‘mechanical complications’’ such as
and CNS (Central Nervous System) Risk Lesions
an uncontrolled pneumothorax [14], or as a late event due to
The findings of the pretreatment clinical evaluation allow defi- chronic emphysematous changes. In the upcoming clinical trial
nition of organ involvement based on the clinical, biological, and for LCH in children (LCH-IV), the lung will be no longer consid-
radiological criteria shown in Table IV. Disease involvement of ered a risk organ.
certain organs is considered as a marker of higher risk of (a) dying Involvement of some skull bones might predispose to diabetes
from disease (risk organs) or (b) developing neuro-degenerative insipidus (DI) and CNS manifestations [15–17]. The term CNS
complications more commonly named as CNS risk lesions. risk lesions, representing a more recent concept [16], suggests that
Risk organs include the hematologic system, the spleen and these patients are more likely to develop neuro-degenerative CNS
the liver (evidence: B, agreement: 2) [8–10]. The lung had been disease, which may be an irreversible complication of LCH and
considered for many decades as a risk organ, but its individual may have a debilitating course [18]. Therefore, skull bone lesions,
prognostic impact has recently been questioned [11]. In fact, in with the exception of the vault, are considered as CNS risk
Pediatr Blood Cancer DOI 10.1002/pbc
4 Haupt et al.

TABLE III. Specific Clinical Scenarios and Recommended Additional Testing in Children With LCH

Clinical scenario and recommended additional testing


History of polyuria or polydipsia
Early morning urine specific gravity and osmolality
Blood electrolytes
Water deprivation test if possible
MRI of the heada
Bicytopenia, pancytopenia, or persistent unexplained single cytopenia
Other causes of anemia or thrombocytopenia has to be ruled out according to standard medical practice. If no other causes are found, the
cytopenia is considered LCH-related
Bone marrow aspirate and trephine biopsy to exclude causes other than LCH b as exposant
Evaluation for features of macrophage activation and hemophagocytic syndrome (triglycerides and ferritin in addition to the coagulation studies
in Table IIac
Liver dysfunction
If frank liver dysfunction (liver enzymes >5-fold upper limit of normal/bilirubin >5-fold upper limit of normal): consult a hepatologist and
consider liver MRI which is preferable to retrograde cholangiography
Liver biopsy is only recommended if there is clinically significant liver involvement and the result will alter treatment (i.e., to differentiate
between active LCH and sclerosing cholangitis)
Lung involvement (further testing is only needed in case of abnormal chest X-ray or symptoms/signs suggestive of lung involvement, or pulmonary
findings not characteristic of LCH or suspicion of an atypical infection)
Lung high resolution computed tomography (HR-CT) or preferably low dose multi-detector HR-CT if available. Note that cysts and nodules are
the only images typical of LCH; all other lesions are not diagnostic. In children already diagnosed with MS-LCH (see section ‘‘Clinical
Classification’’) low dose CT is sufficient in order to assess extent of pulmonary involvement, and reduce the radiation exposure
Lung function tests (if age appropriate)
Bronchoalveolar lavage (BAL): >5% CD1a þ cells in BAL fluid may be diagnostic in a non-smokerd
Lung biopsy (if BAL is not diagnostic)
Suspected craniofacial bone lesions including maxilla and mandible
MRI of heada including the brain, hypothalamus–pituitary axis, and all craniofacial bones. If MRI not available, CT of the involved bone and the
skull base is recommended
Aural discharge or suspected hearing impairment/mastoid involvement
Formal hearing assessment
MRI of heada or HR-CT of temporal bone
Vertebral lesions (even if only suspected)
MRI of spine to assess for soft tissue massess and to exclude spinal cord compression
Visual or neurological abnormalities
MRI of heada
Neurological assessment
Neuropsychometric assessment
Suspected other endocrine abnormality (i.e., short stature, growth failure, hypothalamic syndromes, precocious, or delayed puberty)
Endocrine assessment (including dynamic tests of the anterior pituitary and thyroid)
MRI of heada
Unexplained chronic diarrhea, failure to thrive, or evidence of malabsorption
Endoscopy
Biopsy

(HR-)CT, (high resolution) computed tomography; MRI, magnetic resonance imaging. aSee Appendix 1 for details. b The clinical significance
of CD1a positivity in the bone marrow remains to be proven. An isolated finding of histiocytic infiltration on the bone marrow with no
cytopenia is not a criterion for diagnosis or reactivation [57,58]. cHemophagocytic syndrome with macrophage activation is a common finding
in patients with hematological dysfunction [59,60]. dSee discussion in Refs. [12,13].

lesions, assuming that risk factors for DI can also be considered as hypothalamic-pituitary/central nervous system, or others such as
risk factors of neuro-degenerative changes (evidence C; agree- thyroid or thymus. In MS-LCH, two or more organs, or systems
ment: 1). are involved either with or without involvement of risk organs.

Clinical Classification General Considerations for Treatment


The current classification differentiates between single system Treatment of single-system LCH. Patients with SS-LCH may
disease (SS-LCH) and multisystem disease (MS-LCH), a distinc- be initially referred to a range of medical specialists depending on
tion based on the extent of involvement at diagnosis. In SS-LCH, the localization and presentation of the lesions, thus it is difficult
only one organ or system is involved such as bone (either as a to organize and execute coordinated international trials. This sec-
single bone or more than one bone), skin, lymph node (not tion combines the limited published evidence with the authors’
the draining lymph node of another LCH lesion), lungs, experience (evidence: C, agreement: 1).
Pediatr Blood Cancer DOI 10.1002/pbc
Guidelines for Langerhans Cell Histiocytosis 5

TABLE IV. Definition of Organ Involvement in Langerhans Cell Histiocytosis

Criteria CNS risk lesions Risk organ


Bone involvement
General bone involvement: all radiologically documented lesions, which are not
mentioned below
Craniofacial bone involvement: lesions in the orbital, temporal, mastoid, sphenoidal, Yes
zygomatic, or ethmoidal bones; the maxilla or paranasal sinuses; or cranial fossa; with
intracranial soft tissue extension
Vertebral involvement without soft tissue extension, for example, vertebra plana
Vertebral involvement with intraspinal soft tissue extension or lesions in the odontoid
peg
An abnormality on Tc bone scan or an MRI hypersignal, not correlated with symptoms,
or with an X-ray image is not considered bony disease!
Central nervous system (CNS) involvement Yes
Tumoral: all intracerebral expansive lesions predominantly affecting the brain or
meninges
Neurodegeneration on MRI: MRI imaging compatible with neurodegenerative
diseasea, that is, abnormal signal intensity localized in the dentate nuclei or cerebellum
or cerebral atrophy NOT explained by corticosteroids
Clinical neurodegeneration: presence of suggestive symptoms (either cerebellar
syndrome or learning difficulty) with compatible MRI imaging
Ear involvement
Ear involvement with external otitis, otitis media, or otorrhea Yes
Eye involvement
Orbital involvement with proptosis or exophthalmos Yes
Hematopoietic involvement Yes
Mild (both of the following categories should be present)
Hemoglobin between 10 and 7 g/dl (not due to other causes, e.g., iron deficiency)
Thrombocytopenia with platelets between 100,000 and 20,000/mm3
Severe (both of the following categories should be present)
Hemoglobin <7 g/dl (not due to other causes, e.g., iron deficiency)
Platelets <20,000/mm3
Liver involvement (the patient can show a combination of these symptoms) Yes
Enlargement >3 cm below the costal margin at the mid clavicular line, confirmed by
ultrasound or dysfunction documented by: hyperbilirubinemia >3 times normal
hypoalbuminemia (<30 g/dl), g GT increased >2 times normal, ALT (SGPT)–AST
(SGOT) >3 times normal, ascites, edema, or intra hepatic nodular mass
Lung involvement (Yes)b
Typical imaging (nodules or cysts) on CT scan
Any atypical mass needs to be explored by BAL or biopsy in order to have
histopathological/cytological diagnosis
Mucosa involvement
Oral involvement with lesions in the oral mucosa, gums
Genital or anal involvement
Pituitary involvement
Any pituitary hormone deficiency or tumor appearance in the hypothalamic-pituitary
axis
Skin involvement
Any rash documented by histological examination or any lesion (erythematous and
crusted macules, papules, or nodules, with or without ulceration, or petechiae, or
seborrhea-like picture) compatible with the diagnosis, if LCH is confirmed by biopsy
of another organ
Spleen involvement Yes
>3 cm below the costal margin at the mid clavicular line, confirmed by ultrasound

ALT (SGPT), alanine transaminase (serum glutamic pyruvic transaminase); AST (SGOT), aspartate transaminase (serum glutamic oxaloacetic
transaminase); BAL, bronchoalveolar lavage; CT, computed tomography; MRI, magnetic resonance imaging. aThe term radiological neuro-
degeneration has been coined to describe a certain pattern of MRI findings, but this terminology may be misleading as it does not necessarily
correlate with histopathology. bSee section ‘‘Risk organs.’’

Pediatr Blood Cancer DOI 10.1002/pbc


6 Haupt et al.

Single system unifocal bone involvement (isolated bone Single system skin involvement (isolated cutaneous LCH).
lesions). Unifocal bone lesions are the predominant clinical LCH confined to the skin is rare and accounts for about 5% of
form of LCH. Spontaneous regression may occur, and the clinical the LCH population. It can occur at any age, but is most common
course is probably not greatly influenced by any form of treat- in newborns and infants. In most of these cases LCH tends to
ment. The decision on the most appropriate approach should be regress spontaneously, but progression to MS-LCH is common.
based on clinical symptoms, the size and location of the disease, Therefore, close follow-up and reassessment of the need for treat-
and on any evidence of healing on imaging. Often, simple curet- ment is warranted in all young patients with this disease form.
tage during the diagnostic biopsy will result in healing, and fur- Cutaneous lesions can appear either as isolated nodules or as a
ther intervention may not be necessary [19]. Indications for skin rash; in patients with isolated nodules surgical excision may
additional treatment include involvement of weight-bearing be indicated, but radical surgery is never warranted. In children
bones, imminent spinal cord compression, unacceptable deformi- with a skin rash, topical steroids are often suggested in standard
ty, intense pain, and functional disability. textbooks, but their efficacy has never been proven. Moreover,
Complete excision of bone lesions (curettage) may be indicat- most patients with isolated cutaneous LCH are often diagnosed
ed if the lesion is small (<2 cm) and is combined with the after unsuccessful treatment with topical steroids for other pre-
diagnostic confirmation. However, radical excision of large sumed diagnoses such as eczema [25]. Topical caryolysine (20%
lesions (>5 cm) is not indicated since it increases the size of nitrogen mustard ointment) has been shown to be effective on skin
the bony defect, could prolong the time to healing, and might LCH [26]. Even with potential mutagenesis effect, no secondary
result in permanent skeletal defects. For lesions 2–5 cms in diam- tumor deleterious effect has been reported in relation to this drug
eter, a biopsy and partial curettage is an option. Depending on for this indication. Unfortunately, it is not easily available and
the size and location of the lesion, an intralesional injection of necessitates application by trained personnel.
methylprednisolone may be administered [20] to promote healing In cases of ineffective local therapy or involvement of an
(evidence: C). Immobilization of the limb may need to be consid- extensive area, systemic therapy with steroids (VBL), or oral
ered and discussed with the orthopedic surgeon in rare cases. low dose methotrexate can be used, but the level of evidence is
‘‘Vertebra plana’’ per se is not an indication for an orthopedic low (D) [27–29]. In the most severe cases, treatments, including
corset, and expert physiotherapy assessment should be consid- thalidomide associated with neurological toxicity, pain and
ered; however, temporary immobilization may be required for fatigue [29], azathioprine, or PUVA-therapy which have been
symptomatic relief in the early phases of vertebral involvement. shown to be effective in some adult patients, might also be con-
Patients with temporal bone lesions and recurrent otorrhea, may sidered in children (evidence: D, agreement: 1).
have a secondary cholesteatoma which may need specific treat-
ment [21].
Single System LCH of the Lymph Nodes
In certain functionally critical anatomical sites, such as the
odontoid peg or other vertebral lesions with intraspinal soft tissue This is an extremely rare presentation of LCH [30]. Excision
extension there may be an immediate risk to the patient because biopsy may be the only treatment required for a solitary lymph
of the potential for disease progression and the hazards involved node.
in attempting a biopsy; however, these are exceptional situations, Single system LCH of the lung (primary pulmonary LCH).
and a biopsy should always be considered. Isolated disease in- This rare disease form occurs predominantly in adolescent and
volving functionally critical anatomical sites may justify systemic adult smokers. The impact of systemic therapy is not well docu-
therapy. mented in children, and adult pulmonologists do not consider it as
Because of the potential for development of sequelae, systemic the standard approach [12,13]. Smoking withdrawal is necessary,
therapy is indicated in patients with lesions involving the skull and usually results in significant clinical improvement and often
base, temporal bone, orbits, and vertebral column, where there is complete resolution. However, isolated lung involvement can be
also involvement of the adjacent soft tissues. very challenging due to the risk of acute severe complications
Single system multifocal bone involvement. LCH which such as pneumothorax, or cardiopulmonary arrest. Pneumothora-
presents with only multiple bone lesions at diagnosis (SS-LCH ces should be treated by standard techniques such as drainage and
multifocal bone) usually remains confined to the skeleton, and possibly pleurodesis. Pleurectomy should be avoided as lung
only rarely extends to other organs like the skin and pituitary transplantation may ultimately be considered in patients with
gland. However, the incidence of reported reactivations in cases severe progressive disease. In case of persisting and progressive
of multifocal bone disease is higher than for unifocal bone disease lung disease, systemic therapy with low dose steroids is most
[22–24]. Regardless of the treatment approaches that vary from commonly used, but 2-chlorodeoxyadenosine (2-CdA), and the
observation only to systemic chemotherapy, survival rates combination of VBL and steroids have also been used (evidence:
approaching 100% are reported for this disease form in almost D, agreement: 1).
all the published series. Therefore, the benefit of therapies should Isolated diabetes insipidus and pituitary involvement.
be evaluated in terms of localization and length of disease activi- DI occurs due to involvement of the posterior pituitary (neurohy-
ty, and hence, risk of permanent consequences and quality of life. pophysis) and may become manifest either before, concurrently,
Unfortunately, due to discrepancy in anatomic bone lesions and or after LCH diagnosis. Isolated DI is not considered an indica-
outcome assessment, published data are difficult to compare and tion for systemic therapy per se, except when active disease is
therefore no definitive conclusions can be reached. The most unequivocally documented by the presence of thickening of the
commonly used therapy for multifocal skeletal LCH consists of pituitary stalk or a mass lesion of the hypothalamic-pituitary axis.
steroids and vinblastine (VBL), a relatively non-toxic, and well A lesion of the hypothalamus–pituitary axis is usually considered
tolerated combination. as active if it had local neurological consequences like alteration
Pediatr Blood Cancer DOI 10.1002/pbc
Guidelines for Langerhans Cell Histiocytosis 7

of the visual field or if its volume is increasing on sequential MRI. centre (evidence: D, agreement: 2). Therapeutic options (evi-
In the experience of experts, DI is with few exceptions uniformly dence: C) include combination chemotherapy with cladribine
irreversible, although DDAVP needs may vary. (2-CdA) and cytarabine (Ara-C) [39] or hematopoietic stem cell
There are some earlier anecdotal reports suggesting that treat- transplantation using reduced intensity conditioning regimen [40].
ment with 2-CdA [31], etoposide [32], or radiation [33,34] soon If there is evidence of disease progression in ‘‘non-risk organs,’’
after DI onset may reverse the condition (evidence: D). treatment with 2-CdA as monotherapy [41] or even with further
Brain lesions. In addition to pituitary stalk lesions, any brain, courses of a combination of VBL and steroids should be
or meningeal lesion (except local reaction to a skull vault lesion) considered.
is considered an indication for systemic therapy. The standard
therapy with vinblastine and steroid can be effective in this situa-
Radiotherapy
tion [35] or 2-CdA monotherapy [36].
Treatment of multisystem LCH. As mentioned before, the Most experts in this field would no longer recommend radio-
major clinical challenges of MS-LCH are mortality in young therapy due to the risk of long term sequelae, including the
children with involvement of risk organs, and bouts of reactiva- potential risk of developing a malignant tumor in the field of
tion resulting in morbidity and permanent consequences which the radiotherapy [38]. However, there are some physicians who
can occur in all age groups. Patients with risk organ involvement consider that radiotherapy may be useful for a single bone lesion
are at risk of death, and a poor response to therapy defines a sub- in teenager (evidence: C, agreement: 2).
group with a particularly dismal prognosis. Patients without in-
volvement of risk organs, although not at risk for mortality, need
Neurodegenerative Complications
systemic therapy in order to control the disease activity, reduce
reactivations, and reduce permanent consequences. Several inter- Neurodegenerative complications represent a complex situa-
national protocols for MS-LCH treatment have been designed tion and such patients need to be managed by a multidisciplinary
within the framework of the HS [8–10]. Their main conclusions team. Several therapies have been attempted but with possibly
are (evidence: B, agreement: 2) (i) standard treatment is based on occasional transitory responses. The treatment options include:
steroids and VBL, (ii) Clinical response after the first 6 weeks retinoic acid (evidence: C) [42], combination treatment with vin-
of treatment is a good marker of further disease evolution. (iii) cristine and Ara-C (evidence: C) [43], intravenous immunoglobu-
Prolonged treatment for at least 1 year reduces the risk of disease lin (evidence: D) [44], and cladribine (evidence: D) [45]. To date,
reactivations. intensive therapies have not shown any effect and should thus be
avoided, especially as they may add to the morbidity.
Front Line Treatment and Evaluation of Response
Monitoring and Supportive Care for
Front line treatment of MS-LCH is based on the association of
Permanent Consequences
VBL 6 mg/m2 i.v. weekly bolus for 6 weeks, with prednisone
40 mg/m2/day given orally in three divided doses for 4 weeks Although LCH is predominantly a benign and treatable dis-
and then tapered over the following 2 weeks. After the first ease, it can result in sequelae affecting various tissues involved
6 weeks of treatment, disease status should be reevaluated and [46]. Some may be present at diagnosis, while others may become
treatment continued accordingly. The evaluation of the disease manifest up to years and decades later. It is thus important to
response is usually classified as ‘‘better’’ in case of complete monitor these patients at least until growth is completed and
resolution or regression of the disease, ‘‘worse’’ in case of pro- possibly into adult life. The most common permanent consequen-
gression of the disease, and ‘‘intermediate,’’ in case of stable or ces are endocrine, auditory, and orthopedic. Neurocognitive, pul-
mixed response with new lesions in one site, and regression in monary, and hepatic sequelae are rare but may cause significant
another site. Other evaluation methods have been proposed such morbidity. The recommended investigations and tests are shown
as the disease activity score [37]. in Table V. A scoring system for sequelae has been developed in
In case of a good response (especially in the risk organs) but order to observe the evolution and to standardize the recording of
with some active disease still present in other sites, treatment with such problems [47].
VBL, and steroids should be continued for another 6 weeks with: Endocrine complications. DI is the most frequent endocrin-
VBL 6 mg/m2 i.v. weekly bolus, and prednisone 40 mg/m2/day opathy associated with LCH with a frequency from 15% to 30%
orally in three divided doses for 3 days every week. One or two of cases [30]. It is thus important to investigate thirst and polyuria
intensive courses according to the above mentioned schedule in LCH patients, even many years after the diagnosis of LCH.
should be followed by maintenance therapy for a total duration Growth hormone deficiency is the most frequent anterior pitu-
of up to 12 months with VBL 6 mg/m2 i.v. bolus every 3 weeks, itary hormone loss and occurs in up to 10% of patients. Measure-
and prednisone 40 mg/m2/day orally in three divided doses for ment of height and weight and assessment of puberty is therefore
5 days every 3 weeks and 6 MP at a dose of 50 mg/m2/day is recommended every 6 months or 1 year until growth is completed.
added if risk organ involvement is present. Any child whose growth is below that expected may need to be
investigated as suggested by the consensus guidelines of the GH
Research Society [48].
Second Line Therapy
Other hormone deficiencies may occur. These include delayed
Refractory disease in patients with hematological involvement puberty and rarely panhypopituitarism. Puberty should be
or liver dysfunction is a rare but life-threatening situation [10,38]. assessed according to Tanner stages and need investigation in
We suggest that such patients need to be referred to a specialized the following cases: delayed onset of puberty (B2 >13 years in
Pediatr Blood Cancer DOI 10.1002/pbc
8 Haupt et al.

TABLE V. Recommendations for Follow-Up of Patients With LCH After Diagnosis

Indication Assesment
All patients Routine assessment at clinically appropriate intervals including:
History of thirst, polyuria
Height, weight, pubertal status, neurological assesment
FBC (CBC), ESR, Liver enzymes, Albumin
Bone involvement X-ray oriented to the pathologic area at 6 weeks, 3 and 6 months and then depending on
clinical findings
If vertebral involvement Monitor for scoliosis especially during periods of rapid growth
If jaw involvement Monitor dental development and jaw growth
Pulmonary involvement Spirometry should be performed regularly (every 6–12 months) and if abnormal X-ray
and high resolution computed tomography of chest may be needed
Endocrine involvement
If endocrine signs and symptoms develops See text for indications for endocrine testing and repeat depending on clinical findings
and specialized advice
If proven hypothalamic-pituitary dysfunction Head MRI, repeated after 1 year and then at 2, 4, 7, and 10 years
CNS involvement
If neurological symptoms/signs develops Neuropsychological tests, cerebellar function assessment and MRI of the head; repeat
depending on clinical findings and specialized advice
If tumorous a lesion has been identified in the Repeat head MRI after 6 weeks (in symptomatic patients and those with tumorous lesions)
CNS and 3 months. Further images should be decided on the basis of the results of the first
two examinations
If neurodegenerative findings on MRI, even Repeat head MRI is performed after 1 year and then at 2, 4, 7, and 10 years
without symptoms
Liver involvement Consider ultrasound scan/MRI of liver or cholangiography and repeat depending on
clinical findings and specialized advice
Ear/temporal bone involvement Audiogram at end of treatment and reassessed at start of school and if any new symptoms
develop

CT, computed tomography; MRI, magnetic resonance imaging, CBC, complete blood count; ESR, erytrocyte sedimentation rate; CNS, central
nervous system; DI, diabetes insipidus, ENT: ear nose throat; BAL, broncho-alveolar lavage, GH, growth hormone.

girls, P2, T2 >14 years in boys), delayed onset of period in girls Oral tissue and jaw. Children with involvement of gums and jaw
(>14 years), precocious puberty (B2 <8 years in girls, P2, T2 <9 should be monitored for dental development and growth of the jaw.
years in boys), arrest, or regression of pubertal development. Neurological. Children with multisystem LCH should be reg-
In case of delayed growth/puberty, bone age should be ularly followed up clinically since they are at risk of developing
assessed by X-ray, and anterior pituitary function tests should late neuropsychological sequelae, in particular cerebellar ataxia
be performed to assess secretion of GH, LH, FSH, ACTH, and learning difficulties. In children with relevant history and/or
and thyroid function. If hormone deficiency is confirmed by the abnormal neurological examination, further investigations includ-
stimulation tests, MRI scan of head (Appendix 1) should be ing neuropsychological tests, cerebellar function assessment
performed. Bone mineral density (DEXA) scan needs to be moni- [49,50], and MRI of the head as described in Appendix 1 should
tored in patients with GH deficiency, delayed puberty, or be performed.
panhypopituitarism. Lungs. In those with a history of lung involvement, spirometry
Orthopedic. When several vertebrae are affected, scoliosis should be performed regularly and if abnormal or progressive,
may become manifest later in life, in particular during periods X-ray and computed tomography of chest may be needed. The
of rapid growth such as puberty. Children should be assessed dangers of smoking should be explained and smoking avoided.
clinically at least annually in order to identify any early signs Pulmonary involvement may also lead to respiratory insufficiency
of scoliosis. They should be referred to the orthopedic surgeon in due to fibrosis and emphysema.
order to start preventive physical therapies (e.g., orthopedic cor- Liver. Liver involvement is rare, but can cause serious mor-
set/brace or neck collar) in order to manage this proactively. If bidity. In those with abnormal liver function consider ultrasound
facial bones are affected, facial asymmetry may become manifest scan, MRI of liver, or cholangiography as clinically indicated. A
and reconstructive surgery may be required. subset of young children with liver involvement may subsequently
Hearing. Subjects with involvement of the middle or inner ear develop sclerosing cholangitis that progresses to cirrhosis; treat-
and the temporal bone should be monitored with audiometry ment for these children includes liver transplantation.
at diagnosis and at end of treatment and reassessed at start of
school and if any new symptoms develop. Early diagnosis and Associated Malignancies
interventional strategies such as hearing aids can avoid deteriora-
tion of school performance and significantly improve learning There is a recognized association between LCH and malignan-
outcome. cies [17]. The malignancies may precede, occur concurrently or
Pediatr Blood Cancer DOI 10.1002/pbc
Guidelines for Langerhans Cell Histiocytosis 9

follow the diagnosis of LCH and should be considered at every 4 Istituto G. Gaslini, Genova, Italy. Riccardo Haupt, MD, Associ-
clinical visit. Acute lymphoblastic leukemia and lymphoma more ated Partner, 5 Johns Hopkins, Baltimore, Maryland, USA. Robert
often occur prior to the diagnosis of LCH but may be diagnosed J. Arceci, MD, PhD, Collaborating Partner, 6 Azienda Ospeda-
within 5 years after LCH. Myeloid leukemias usually follow LCH liero-Universitaria Meyer, Firenze, Italy. Maurizio Aricò, MD,
especially in those patients exposed to etoposide, alkylating PhD, Collaborating Partner, 7 Elisabethinen Hospital, Linz,
agents and/or radiotherapy. Solid tumors may occur concurrently Austria. Michael Girschikofsky, MD, Collaborating Partner, 8
or follow the diagnosis of LCH. Most of those that followed LCH Karolinska Institutet, Stockholm, Sweden. Jan-Inge Henter, MD,
developed in a previous radiation field. With the current treatment PhD, Collaborating Partner, 9 Children’s University Hospital,
strategies it is expected that these types of secondary malignancy Hamburg, Germany. Gritta Janka, MD, PhD, Collaborating Part-
will be rare. Patients treated with radiotherapy should see their ner, 10 Hotel Dieu de France Hospital, Beirut, Lebanon. Claudia
doctor in case of symptoms involving the irradiated area. Djambas Khayat, MD, Collaborating Partner, 11 Hellenic Air
Force & Veterans General Hospital, Athens, Greece. Polyzois
Makras, MD, PhD, Collaborating Partner, 12 Hospital de Clı́nicas
Follow-Up/Duration and Frequency
de Porto Alegre, Brasil. Mariana Michalowski, MD, Collaborating
Recommendations for follow-up are shown in Table V. They Partner, 13 Watford General Hospital, Watford, UK. Vasanta
are inspired by the long term follow-up for childhood cancer Nanduri, MD, Collaborating Partner, 14 Dana Farber Cancer In-
survivors [51,52]. Every patient should be followed by the local stitute and Childrens Hospital, Boston, Massachusetts, USA. Car-
physician and if at any time a particular issue needs to be los Rodriguez-Galindo, MD, Collaborating Partner, 15 Medical
addressed, referral to a specialist is recommended. All patients University Plovdiv, Bulgaria. Mariya Spasova, MD, PhD, Associ-
should be followed for a sufficient time period, defined as (i) at ate Professor, Collaborating Partner, 16 University Pediatric
least 5 years after the end of therapy; or (ii) 5 years after the last Hospital, Lublin, Poland. Maria Jolanta Stefaniak, MD, PhD,
disease reactivation, in those who did not receive systemic thera- Collaborating Partner, 17 UZ Leuven, Leuven, Belgium. Stefaan
py; or (iii) until final growth and pubertal development have Van Gool, MD, PhD, Collaborating Partner, 18 University Hos-
occurred. pitals of Leicester, Leicester Royal Infirmary Childrens Hospital,
Perspectives. LCH is a rare disease potentially resulting in Leicester, United Kingdom. Johann Visser, MD, Collaborating
death or permanent sequelae. The burden of therapy may also Partner, 19 Hospital for Sick Children, Toronto, Ontario, Canada.
be extremely heavy. There is an obvious need for a full assess- Sheila Weitzman, MD, Collaborating Partner, 20 Newcastle Uni-
ment of each patient with a rational treatment tailored to the risks versity, Newcastle, United Kingdom. Kevin Patrick Windebank,
of the individual patient, which contributes to further fundamental MD, Collaborating Partner, 21 Clinique Al Madina, Casablanca,
and clinical research in this field. Morocco. Saadia Zafad, MD, PhD, Collaborating Partner.
In 2010, Badalian-Very et al. [53], reported somatic mutations Euro Histio Net Partners—Patient Associations. 1 The His-
of the BRAF oncogene in about half of the LCH patients in their tiocytosis Research Trust, United Kingdom, www.hrtrust.org As-
series, and this finding was recently confirmed by other teams sociated Partner; 2 Artemis Association on Histiocytoses, Greece,
[54,55]. This discovery may have a significant potential impact if www.histioartemis.gr Collaborating Partner; 3 Asociacion Espa-
we consider the possibility of treating LCH with the new class of nola contra la Histiocitosis de celulas de Langerhans (ACHE),
BRAF inhibitors. However, this promising discovery will need to Spain, www.histiocitosis.org Collaborating Partner; 4 Association
be verified and concretized before these drugs can be used for Histiocytose France (A.H.F.), France, www.histiocytose.org Col-
treatment of LCH. The group(s) of LCH patients who may benefit laborating Partner; 5 Associazione italiana ricerca istiocitosi
from BRAF inhibitor treatment must be determined and balanced (AIRI LCH onlus), Italy, www.istiocitosi.org Collaborating Part-
with toxicities as in the case of melanoma [56,57]. Knowledge ner; 6 Erwachsenen Histiozytose X e.V (EHX e.V.)., Germany,
about drug schedule and safety, especially long-term effects [57] www.histiozytose.com Collaborating Partner; 7 Föräldraförenin-
and mechanisms of resistance [58] must be acquired. gen För Histiocytos (Ffh), Sweden, www.histiocytos.se Collabo-
Progress may be expected from collaborations organized at rating Partner; 8 Histiocytosis Association of America (HAA),
national and international levels, among specialist groups and USA, www.histio.org Collaborating Partner; 9 Histiozytosehilfe
expert networks. Collection of tissue and blood samples in bio- e.V., Germany, www.histiozytose.org Collaborating Partner;
banks is essential for improving the understanding of the biology 10 LCH-Belgium, Belgium, www.lch.be Collaborating Partner;
of this rare and fascinating condition. New international protocols 11 The ECD Global Alliance, USA, www.erdheim-chester.org
will soon be opened and continue to represent an opportunity to Collaborating Partner.
develop global research in LCH (see www.histiocytesociety.org
and www.histio.net).
Euro Histio Net Partners—Institutions. Euro Histio Net is REFERENCES
a project funded by the European Commission/DG Sanco and 1. Guyatt GH, Oxman AD, Vist GE, et al. GRADE: An emerging consensus on rating quality of evidence
associated both medical institutions and patients associations as and strength of recommendations. BMJ 2008;336:924–926.
2. Guyatt GH, Oxman AD, Sultan S, et al. GRADE guidelines: 9. Rating up the quality of evidence.
listed below. 1 Reference Centre for Histiocytosis, Hopital Trous- J Clin Epidemiol 2011;64:1311–1316.
seau, Assistance Publique – Hopitaux de Paris, France. Jean 3. Chikwava K, Jaffe R. Langerin (CD207) staining in normal pediatric tissues, reactive lymph nodes, and
childhood histiocytic disorders. Pediatr Dev Pathol 2004;7:607–614.
Donadieu, MD, PhD, Coordinator, Abdelatif Tazi, MD, PhD, 4. Lau SK, Chu PG, Weiss LM. Immunohistochemical expression of Langerin in Langerhans cell
Jean François Emile, MD, PhD, Milen Minkov, MD, PhD, Asso- histiocytosis and non-Langerhans cell histiocytic disorders. Am J Surg Pathol 2008;32:615–619.
5. Swerdlow SH, Campo E, Harris NL, et al. WHO classification of tumours of haematopoietic and
ciated Partners, 2 Hospital Universitario Cruces Barakaldo, Spain. lymphoid tissues, 4th edition. Lyon: IARC press; 2008.
6. Valladeau J, Ravel O, zutter-Dambuyant C, et al. Langerin, a novel C-type lectin specific to Langer-
Itziar Astigarraga, MD, Associated Partner, 3 Children’s Cancer hans cells, is an endocytic receptor that induces the formation of Birbeck granules. Immunity
Research Institute, St. Anna Children’s Hospital, Vienna, Austria. 2000;12:71–81.

Pediatr Blood Cancer DOI 10.1002/pbc


10 Haupt et al.
7. Jaffe R. The diagnostic histopathology of Langerhans cell histiocytosis. In: Weitzman S, Egeler M, 36. Dhall G, Finlay JL, Dunkel IJ, et al. Analysis of outcome for patients with mass lesions of the central
editors. Histiocytic disorders of children and adults. Cambridge, UK: Cambridge University Press; nervous system due to Langerhans cell histiocytosis treated with 2-chlorodeoxyadenosine. Pediatr
2005. pp. 14–39. Blood Cancer 2008;50:72–79.
8. Gadner H, Grois N, Arico M, et al. A randomized trial of treatment for multisystem Langerhans’ cell 37. Donadieu J, Piguet C, Bernard F, et al. A new clinical score for disease activity in Langerhans cell
histiocytosis. J Pediatr 2001;138:728–734. histiocytosis. Pediatr Blood Cancer 2004;43:770–776.
9. Gadner H, Grois N, Potschger U, et al. Improved outcome in multisystem Langerhans cell histiocytosis 38. The French Langerhans’ Cell Histiocytosis Study Group. A multicentre retrospective survey of
is associated with therapy intensification. Blood 2007;111:2556–2562. Langerhans’ cell histiocytosis : 348 cases observed between 1983 and 1993. Arch Dis Child 1996;
10. Minkov M, Grois N, Heitger A, et al. Response to initial treatment of multisystem Langerhans cell 75:17–24.
histiocytosis: An important prognostic indicator. Med Pediatr Oncol 2002;39:581–585. 39. Bernard F, Thomas C, Bertrand Y, et al. Multi-centre pilot study of 2-chlorodeoxyadenosine and
11. Ronceray L, Potschger U, Janka G, et al. Pulmonary involvement in pediatric-onset multisystem cytosine arabinoside combined chemotherapy in refractory Langerhans cell histiocytosis with haema-
langerhans cell histiocytosis: Effect on course and outcome. J Pediatr 2012;161:129–133. tological dysfunction. Eur J Cancer 2005;41:2682–2689.
12. Tazi A, Soler P, Hance AJ. Adult pulmonary Langerhans’ cell histiocytosis. Thorax 2000;55:405–416. 40. Steiner M, Matthes-Martin S, Attarbaschi A, et al. Improved outcome of treatment-resistant high-risk
13. Vassallo R, Ryu JH, Colby TV, et al. Pulmonary Langerhans’-cell histiocytosis. N Engl J Med Langerhans cell histiocytosis after allogeneic stem cell transplantation with reduced-intensity condi-
2000;342:1969–1978. tioning. Bone Marrow Transplant 2005;36:215–225.
14. Braier J, Latella A, Balancini B, et al. Outcome in children with pulmonary Langerhans cell histio- 41. Weitzman S, Braier J, Donadieu J, et al. 20 -Chlorodeoxyadenosine (2-CdA) as salvage therapy for
cytosis. Pediatr Blood Cancer 2004;43:765–769. Langerhans cell histiocytosis (LCH). Results of the LCH-S-98 protocol of the histiocyte society.
15. Donadieu J, Rolon MA, Thomas C, et al. Endocrine involvement in pediatric-onset Langerhans’ cell Pediatr Blood Cancer 2009;53:1271–1276.
histiocytosis: A population-based study. J Pediatr 2004;144:344–350. 42. Idbaih A, Donadieu J, Barthez MA, et al. Retinoic acid therapy in ‘‘degenerative-like’’ neuro-
16. Grois N, Potschger U, Prosch H, et al. Risk factors for diabetes insipidus in Langerhans cell histio- Langerhans cell histiocytosis: A prospective pilot study. Pediatr Blood Cancer 2004;43:55–58.
cytosis. Pediatr Blood Cancer 2006;46:228–233. 43. Allen CE, Flores R, Rauch R, et al. Neurodegenerative central nervous system Langerhans cell
17. Haupt R, Nanduri VR, Egeler RM. Late effects of Langerhans cell histiocytosis and the association of histiocytosis and coincident hydrocephalus treated with vincristine/cytosine arabinoside. Pediatr Blood
LCH with malignancy. In: Egeler RM, Weitzman S, editor. Histiocytic disorders in children and adults. Cancer 2009;54:416–423.
Cambridge, UK: Cambridge University Press; 2005. 44. Gavhed D, Laurencikas E, Akefeldt SO, et al. Fifteen years of treatment with intravenous immuno-
18. Grois N, Fahrner B, Arceci RJ, et al. Central nervous system disease in Langerhans cell histiocytosis. globulin in central nervous system Langerhans cell histiocytosis. Acta Paediatr 2011;100:e36–e39.
J Pediatr 2010;156:873–881, 881. 45. Buchler T, Cervinek L, Belohlavek O, et al. Langerhans cell histiocytosis with central nervous system
19. Berry DH, Gresik M, Maybee D, et al. Histiocytosis X in bone only. Med Pediatr Oncol 1990;18: involvement: Follow-up by FDG-PET during treatment with cladribine. Pediatr Blood Cancer
292–294. 2005;44:286–288.
20. Egeler RM, Thompson RC, Jr., Voute PA, et al. Intralesional infiltration of corticosteroids in localized 46. Haupt R, Nanduri V, Calevo MG, et al. Permanent consequences in Langerhans cell histiocytosis
Langerhans’ cell histiocytosis. J Pediatr Orthop 1992;12:811–814. patients: A pilot study from the Histiocyte Society-Late Effects Study Group. Pediatr Blood Cancer
21. Roger G, Dupre M, Leboulanger N, et al. Cholesteatoma secondary to temporal bone involvement 2004;42:438–444.
by Langerhans cell histiocytosis: A complication amenable to curative surgery. Otol Neurotol 47. Nanduri VR, Pritchard J, Levitt G, et al. Long term morbidity and health related quality of life after
2009;30:190–193. multi-system Langerhans cell histiocytosis. Eur J Cancer 2006;42:2563–2569.
22. Dimentberg RA, Brown KL. Diagnostic evaluation of patients with histiocytosis X. J Pediatr Orthop 48. GH Research Society. Consensus guidelines for the diagnosis and treatment of growth hormone (GH)
1990;10:733–741. deficiency in childhood and adolescence: Summary statement of the GH Research Society. GH
23. Raney RB, Jr., D’Angio GJ. Langerhans’ cell histiocytosis (histiocytosis X): Experience at the Child- Research Society. J Clin Endocrinol Metab 2000;85:3990–3993.
ren’s Hospital of Philadelphia, 1970–1984. Med Pediatr Oncol 1989;17:20–28. 49. Schmahmann JD, Gardner R, MacMore J, et al. Development of a brief ataxia rating scale (BARS)
24. Sessa S, Sommelet D, Lascombes P, et al. Treatment of Langerhans-cell histiocytosis in children. based on a modified form of the ICARS. Mov Disord 2009;24:1820–1828.
Experience at the Children’s Hospital of Nancy. J Bone Joint Surg Am 1994;76:1513–1525. 50. Trouillas P, Takayanagi T, Hallett M, et al. International Cooperative Ataxia Rating Scale for pharma-
25. Krafchik B, Pope E, Walsh SRA. Histiocytosis of the skin in children and adults. In: Weitzman S, cological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the
Egeler M, editors. Histiocytic disorders of children and adults. Cambridge, UK: Cambridge University World Federation of Neurology. J Neurol Sci 1997;145:205–211.
Press; 2005. pp. 130–153. 51. Curry HL, Parkes SE, Powell JE, et al. Caring for survivors of childhood cancers: The size of the
26. Hadfield PJ, Birchall MA, Albert DM. Otitis externa in Langerhans’ cell histiocytosis—The successful problem. Eur J Cancer 2006;42:501–508.
use of topical nitrogen mustard. Int J Pediatr Otorhinolaryngol 1994;30:143–149. 52. Kenney LB, Bradeen H, Kadan-Lottick NS, et al. The current status of follow-up services for
27. Steen AE, Steen KH, Bauer R, et al. Successful treatment of cutaneous Langerhans cell histiocytosis childhood cancer survivors, are we meeting goals and expectations: A report from the Consortium
with low-dose methotrexate. Br J Dermatol 2001;145:137–140. for New England Childhood Cancer Survivors. Pediatr Blood Cancer 2011;57:1062–1066.
28. Womer RB, Anunciato KR, Chehrenama M. Oral methotrexate and alternate-day prednisone for low- 53. Badalian-Very G, Vergilio JA, Degar BA, et al. Recurrent BRAF mutations in Langerhans cell
risk Langerhans cell histiocytosis. Med Pediatr Oncol 1995;25:70–73. histiocytosis. Blood 2010;116:1919–1923.
29. McClain KL, Kozinetz CA. A phase II trial using thalidomide for Langerhans cell histiocytosis. Pediatr 54. Satoh T, Smith A, Sarde A, et al. B-RAF mutant alleles associated with Langerhans cell histiocytosis, a
Blood Cancer 2007;48:44–49. granulomatous pediatric disease. PLoS ONE 2012;7:e33891.
30. Donadieu J, Egeler M, Pritchard J. Langerhans cell histiocytosis: A clinical update. In: Weitzman S, 55. Haroche J, Charlotte F, Arnaud L, et al. High prevalence of BRAF V600E mutations in Erdheim–
Egeler M, editors. Histiocytic disorders of children and adults. Cambridge, UK: Cambridge University Chester disease but not in other non-Langerhans cell histiocytoses. Blood 2012;120:2700–2703.
Press; 2005. pp. 95–129. 56. Phillips M, Allen C, Gerson P, et al. Comparison of FDG-PET scans to conventional radiography
31. Ottaviano F, Finlay JL. Diabetes insipidus and Langerhans cell histiocytosis: A case report of revers- and bone scans in management of Langerhans cell histiocytosis. Pediatr Blood Cancer 2009;52:
ibility with 2-chlorodeoxyadenosine. J Pediatr Hematol Oncol 2003;25:575–577. 97–101.
32. Broadbent V, Pritchard J. Diabetes insipidus associated with Langerhans cell histiocytosis: Is it 57. McClain K, Ramsay NK, Robison L, et al. Bone marrow involvement in histiocytosis X. Med Pediatr
reversible? Med Pediatr Oncol 1997;28:289–293. Oncol 1983;11:167–171.
33. Minehan KJ, Chen MG, Zimmerman D, et al. Radiation therapy for diabetes insipidus caused by 58. Minkov M, Potschger U, Grois N, et al. Bone marrow assessment in Langerhans cell histiocytosis.
Langerhans cell histiocytosis. Int J Radiat Oncol Biol Phys 1992;23:519–524. Pediatr Blood Cancer 2007;49:694–698.
34. Rosenzweig KE, Arceci RJ, Tarbell NJ. Diabetes insipidus secondary to Langerhans’ cell histiocytosis: 59. Favara BE, Jaffe R, Egeler RM. Macrophage activation and hemophagocytic syndrome in Langerhans
Is radiation therapy indicated? Med Pediatr Oncol 1997;29:36–40. cell histiocytosis: Report of 30 cases. Pediatr Dev Pathol 2002;5:130–140.
35. Ng Wing TS, Martin-Duverneuil N, Idbaih A, et al. Efficacy of vinblastine in central nervous system 60. Galluzzo ML, Braier J, Rosenzweig SD, et al. Bone marrow findings at diagnosis in patients with
Langerhans cell histiocytosis: A nation wide retrospective study. Orphanet J Rare Dis 2011;6:83. multisystem Langerhans cell histiocytosis. Pediatr Dev Pathol 2010;13:101–106.

Pediatr Blood Cancer DOI 10.1002/pbc